Harold Riethman

7.8k total citations
68 papers, 3.7k citations indexed

About

Harold Riethman is a scholar working on Molecular Biology, Plant Science and Physiology. According to data from OpenAlex, Harold Riethman has authored 68 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 38 papers in Plant Science and 22 papers in Physiology. Recurrent topics in Harold Riethman's work include Chromosomal and Genetic Variations (37 papers), Telomeres, Telomerase, and Senescence (20 papers) and Genomic variations and chromosomal abnormalities (16 papers). Harold Riethman is often cited by papers focused on Chromosomal and Genetic Variations (37 papers), Telomeres, Telomerase, and Senescence (20 papers) and Genomic variations and chromosomal abnormalities (16 papers). Harold Riethman collaborates with scholars based in United States, United Kingdom and Germany. Harold Riethman's co-authors include Louis A. Sherman, Zhong Deng, Paul M. Lieberman, Andreas Wiedmer, Julie Norseen, Maynard V. Olson, Anthony E. Ambrosini, Eric D. Green, Jonathan Flint and David H. Ledbetter and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Harold Riethman

68 papers receiving 3.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Harold Riethman United States 33 2.4k 1.1k 1.1k 1.1k 242 68 3.7k
James B. Stewart Germany 38 4.5k 1.8× 952 0.9× 256 0.2× 230 0.2× 102 0.4× 60 5.3k
Peter Baumann United States 40 4.6k 1.9× 990 0.9× 731 0.7× 1.9k 1.8× 26 0.1× 91 6.3k
N D Hastie United Kingdom 23 2.7k 1.1× 738 0.7× 421 0.4× 1.4k 1.3× 208 0.9× 31 4.0k
E. Viégas-Pèquignot France 33 4.2k 1.7× 2.0k 1.8× 810 0.7× 284 0.3× 587 2.4× 92 6.0k
Michael Kessel Germany 38 4.6k 1.9× 1.7k 1.6× 180 0.2× 182 0.2× 180 0.7× 138 6.2k
Katia Ancelin France 17 3.1k 1.3× 844 0.8× 355 0.3× 667 0.6× 143 0.6× 29 3.6k
Bernard Maro France 49 5.3k 2.2× 826 0.8× 750 0.7× 142 0.1× 626 2.6× 102 7.9k
Predrag Slijepčević United Kingdom 27 1.7k 0.7× 338 0.3× 640 0.6× 1.2k 1.1× 51 0.2× 89 2.6k
Rolf Jessberger Germany 47 4.5k 1.8× 943 0.9× 1.0k 0.9× 304 0.3× 625 2.6× 118 7.1k
Karl Illmensee Switzerland 30 3.1k 1.3× 1.5k 1.3× 267 0.2× 123 0.1× 176 0.7× 85 4.8k

Countries citing papers authored by Harold Riethman

Since Specialization
Citations

This map shows the geographic impact of Harold Riethman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Harold Riethman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Harold Riethman more than expected).

Fields of papers citing papers by Harold Riethman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Harold Riethman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Harold Riethman. The network helps show where Harold Riethman may publish in the future.

Co-authorship network of co-authors of Harold Riethman

This figure shows the co-authorship network connecting the top 25 collaborators of Harold Riethman. A scholar is included among the top collaborators of Harold Riethman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Harold Riethman. Harold Riethman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Young, Eleanor, et al.. (2020). Comprehensive Analysis of Human Subtelomeres by Whole Genome Mapping. PLoS Genetics. 16(1). e1008347–e1008347. 25 indexed citations
2.
Young, Eleanor, et al.. (2020). Single-molecule telomere length characterization by optical mapping in nano-channel array: Perspective and review on telomere length measurement. Environmental Toxicology and Pharmacology. 82. 103562–103562. 4 indexed citations
3.
Ranjan, Desh, et al.. (2019). Analysis of Subtelomeric REXTAL Assemblies Using QUAST. IEEE/ACM Transactions on Computational Biology and Bioinformatics. 18(1). 365–372. 3 indexed citations
4.
Lynch, Shannon M., M. Kristen Peek, Nandita Mitra, et al.. (2016). Race, Ethnicity, Psychosocial Factors, and Telomere Length in a Multicenter Setting. PLoS ONE. 11(1). e0146723–e0146723. 57 indexed citations
5.
McCaffrey, Jennifer, Justin Sibert, Bin Zhang, et al.. (2015). CRISPR-CAS9 D10A nickase target-specific fluorescent labeling of double strand DNA for whole genome mapping and structural variation analysis. Nucleic Acids Research. 44(2). e11–e11. 40 indexed citations
6.
Sedic, Maja, Adam Skibinski, Nelson E. Brown, et al.. (2015). Haploinsufficiency for BRCA1 leads to cell-type-specific genomic instability and premature senescence. Nature Communications. 6(1). 7505–7505. 94 indexed citations
7.
Stong, Nicholas, Zhong Deng, Ravi Gupta, et al.. (2014). Subtelomeric CTCF and cohesin binding site organization using improved subtelomere assemblies and a novel annotation pipeline. Genome Research. 24(6). 1039–1050. 51 indexed citations
8.
Deng, Zhong, Julie Norseen, Andreas Wiedmer, Harold Riethman, & Paul M. Lieberman. (2009). TERRA RNA Binding to TRF2 Facilitates Heterochromatin Formation and ORC Recruitment at Telomeres. Molecular Cell. 35(4). 403–413. 429 indexed citations
9.
Ambrosini, Anthony E., et al.. (2007). Human subtelomeric duplicon structure and organization. Genome biology. 8(7). R151–R151. 42 indexed citations
10.
Riethman, Harold, et al.. (2005). Human subtelomere structure and variation. Chromosome Research. 13(5). 505–515. 88 indexed citations
11.
Riethman, Harold, et al.. (2001). Integration of telomere sequences with the draft human genome sequence. Nature. 409(6822). 948–951. 63 indexed citations
12.
Knight, Samantha J.L., Christa M. Lese, Kathrin S. Precht, et al.. (2000). An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture. The American Journal of Human Genetics. 67(2). 320–332. 237 indexed citations
13.
Negorev, Dmitri, Harold Riethman, Robert J. Wechsler‐Reya, et al.. (1996). The Bin1 Gene Localizes to Human Chromosome 2q14 by PCR Analysis of Somatic Cell Hybrids and Fluorescencein SituHybridization. Genomics. 33(2). 329–331. 24 indexed citations
14.
Macina, Roberto A., et al.. (1995). Molecular cloning and RARE cleavage mapping of human 2p, 6q, 8q, 12q, and 18q telomeres.. Genome Research. 5(3). 225–232. 23 indexed citations
15.
Martín-Gallardo, Antonia, Jane E. Lamerdin, Cynthia Friedman, et al.. (1995). Molecular analysis of a novel subtelomeric repeat with polymorphic chromosomal distribution. Cytogenetic and Genome Research. 71(3). 289–295. 25 indexed citations
16.
Macina, Roberto A., Frederic G. Barr, Naomi Galili, & Harold Riethman. (1995). Genomic organization of the human PAX3 gene: DNA sequence analysis of the region disrupted in alveolar rhabdomyosarcoma. Genomics. 26(1). 1–8. 33 indexed citations
17.
Negorev, Dmitri, et al.. (1994). Physical Analysis of the Terminal 270 kb of DNA from Human Chromosome 1q. Genomics. 22(3). 569–578. 13 indexed citations
18.
19.
Macina, Roberto A. & Harold Riethman. (1992). Direct DNA hybridization screening of primary yeast transformants in the construction of targeted Yeast Artificial Chromosome (YAC) libraries. Genetic Analysis Biomolecular Engineering. 9(2). 58–63. 1 indexed citations
20.
Lengauer, Christoph, Harold Riethman, & Thomas Cremer. (1990). Painting of human chromosomes with probes generated from hybrid cell lines by PCR with Alu and L1 primers. Human Genetics. 86(1). 1–6. 53 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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